Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:22200452n
Noun Concept
AR
No term available
EN
The Emberger syndrome is a rare, autosomal dominant, genetic disorder caused by familial or sporadic inactivating mutations in one of the two parental GATA2 genes. Wikipedia
Relations
Sources
IS A
مرض
مرض نادر
سرطان الرأس والعنق
أورام الأنسجة المكونة للدم والأنسجة الليمفاوية
GENETIC ASSOCIATION
EN
GATA2

Please note that, in order to improve your browsing experience on this website, BabelNet® uses various types of cookies, including: browsing functionality, performance and statistical cookies.

By continuing to browse the site you are agreeing to our use of cookies. OK

License